A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035440



Internal ID21944783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113726065..113726121hg38UCSC Ensembl
chr13:114429038..114429094hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603151
Samples
Known GenesGRK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035440
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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